A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973397



Internal ID22748333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51099419..51103756hg38UCSC Ensembl
chrX:50842265..50846602hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg384338
hg194338
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973397
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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